GB1428436A - Method for producing biologically tolerated polymers - Google Patents
Method for producing biologically tolerated polymersInfo
- Publication number
- GB1428436A GB1428436A GB2393873A GB2393873A GB1428436A GB 1428436 A GB1428436 A GB 1428436A GB 2393873 A GB2393873 A GB 2393873A GB 2393873 A GB2393873 A GB 2393873A GB 1428436 A GB1428436 A GB 1428436A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymers
- methacrylate
- examples
- hydroxy
- blocked
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 title abstract 5
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 abstract 3
- 150000002440 hydroxy compounds Chemical class 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 150000001993 dienes Chemical class 0.000 abstract 2
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 230000007246 mechanism Effects 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- -1 #-vinylacrylic acid Chemical compound 0.000 abstract 1
- MEIRRNXMZYDVDW-MQQKCMAXSA-N (2E,4E)-2,4-hexadien-1-ol Chemical compound C\C=C\C=C\CO MEIRRNXMZYDVDW-MQQKCMAXSA-N 0.000 abstract 1
- ACZNIBVNGPLHAC-ONEGZZNKSA-N (2e)-penta-2,4-dien-1-ol Chemical compound OC\C=C\C=C ACZNIBVNGPLHAC-ONEGZZNKSA-N 0.000 abstract 1
- MBVAQOHBPXKYMF-LNTINUHCSA-N (z)-4-hydroxypent-3-en-2-one;rhodium Chemical compound [Rh].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O MBVAQOHBPXKYMF-LNTINUHCSA-N 0.000 abstract 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 abstract 1
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 abstract 1
- OLQFXOWPTQTLDP-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCO OLQFXOWPTQTLDP-UHFFFAOYSA-N 0.000 abstract 1
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 abstract 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 abstract 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 abstract 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 abstract 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 abstract 1
- XYFRHHAYSXIKGH-UHFFFAOYSA-N 3-(5-methoxy-2-methoxycarbonyl-1h-indol-3-yl)prop-2-enoic acid Chemical compound C1=C(OC)C=C2C(C=CC(O)=O)=C(C(=O)OC)NC2=C1 XYFRHHAYSXIKGH-UHFFFAOYSA-N 0.000 abstract 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 abstract 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- CWXPWGARSHBQBS-UHFFFAOYSA-N bis(ethenyl)-methoxysilane Chemical compound CO[SiH](C=C)C=C CWXPWGARSHBQBS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004566 building material Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- FJDJVBXSSLDNJB-LNTINUHCSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical compound [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FJDJVBXSSLDNJB-LNTINUHCSA-N 0.000 abstract 1
- SAXCKUIOAKKRAS-UHFFFAOYSA-N cobalt;hydrate Chemical compound O.[Co] SAXCKUIOAKKRAS-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004132 cross linking Methods 0.000 abstract 1
- ATMMGNJQKWCZTH-UHFFFAOYSA-N deca-7,9-diene-2,3-diol Chemical compound C=CC=CCCCC(C(C)O)O ATMMGNJQKWCZTH-UHFFFAOYSA-N 0.000 abstract 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 abstract 1
- 235000013305 food Nutrition 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 238000001631 haemodialysis Methods 0.000 abstract 1
- 210000003709 heart valve Anatomy 0.000 abstract 1
- DJNZIOMNORCXHM-UHFFFAOYSA-N hepta-4,6-dien-3-ol Chemical compound CCC(O)C=CC=C DJNZIOMNORCXHM-UHFFFAOYSA-N 0.000 abstract 1
- SZYLTIUVWARXOO-UHFFFAOYSA-N hexa-1,5-dien-3-ol Chemical compound C=CC(O)CC=C SZYLTIUVWARXOO-UHFFFAOYSA-N 0.000 abstract 1
- 239000007943 implant Substances 0.000 abstract 1
- KCWDJXPPZHMEIK-UHFFFAOYSA-N isocyanic acid;toluene Chemical compound N=C=O.N=C=O.CC1=CC=CC=C1 KCWDJXPPZHMEIK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000012528 membrane Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000003607 modifier Substances 0.000 abstract 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 abstract 1
- FJCZSUYRNVRTFV-UHFFFAOYSA-N octa-4,6-dien-3-ol Chemical compound CCC(O)C=CC=CC FJCZSUYRNVRTFV-UHFFFAOYSA-N 0.000 abstract 1
- ICMWSAALRSINTC-UHFFFAOYSA-N penta-1,4-dien-3-ol Chemical compound C=CC(O)C=C ICMWSAALRSINTC-UHFFFAOYSA-N 0.000 abstract 1
- RGBXDEHYFWDBKD-UHFFFAOYSA-N propan-2-yl propan-2-yloxy carbonate Chemical compound CC(C)OOC(=O)OC(C)C RGBXDEHYFWDBKD-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 238000001223 reverse osmosis Methods 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
- BLNCHCHRIQHWNH-UHFFFAOYSA-N trimethyl(penta-2,4-dienoxy)silane Chemical compound C[Si](C)(C)OCC=CC=C BLNCHCHRIQHWNH-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Materials For Medical Uses (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Eyeglasses (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS422172A CS161327B1 (cs) | 1972-06-16 | 1972-06-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1428436A true GB1428436A (en) | 1976-03-17 |
Family
ID=5384460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2393873A Expired GB1428436A (en) | 1972-06-16 | 1973-05-18 | Method for producing biologically tolerated polymers |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JPS4952281A (cs) |
| AU (1) | AU477290B2 (cs) |
| CA (1) | CA1045296A (cs) |
| CH (1) | CH583756A5 (cs) |
| CS (1) | CS161327B1 (cs) |
| DE (1) | DE2325169A1 (cs) |
| FR (1) | FR2189431B1 (cs) |
| GB (1) | GB1428436A (cs) |
| IT (1) | IT987928B (cs) |
| NL (1) | NL7307697A (cs) |
| SE (1) | SE396953B (cs) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2125685A (en) * | 1935-03-16 | 1938-08-02 | Ig Farbenindustrie Ag | Polymerization products and process of preparing them |
| US3041320A (en) * | 1961-05-01 | 1962-06-26 | Monsanto Chemicals | Copolymers of 2-hydroxymethyl butadienes and 1, 3-dienes |
-
1972
- 1972-06-16 CS CS422172A patent/CS161327B1/cs unknown
-
1973
- 1973-05-18 DE DE19732325169 patent/DE2325169A1/de active Pending
- 1973-05-18 GB GB2393873A patent/GB1428436A/en not_active Expired
- 1973-05-25 IT IT2463873A patent/IT987928B/it active
- 1973-06-01 NL NL7307697A patent/NL7307697A/xx not_active Application Discontinuation
- 1973-06-04 CH CH810673A patent/CH583756A5/xx not_active IP Right Cessation
- 1973-06-04 JP JP48062065A patent/JPS4952281A/ja active Pending
- 1973-06-04 SE SE7308401A patent/SE396953B/xx unknown
- 1973-06-15 FR FR7321819A patent/FR2189431B1/fr not_active Expired
- 1973-06-15 CA CA174,171A patent/CA1045296A/en not_active Expired
- 1973-06-18 AU AU57024/73A patent/AU477290B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CS161327B1 (cs) | 1975-06-10 |
| CH583756A5 (cs) | 1977-01-14 |
| JPS4952281A (cs) | 1974-05-21 |
| DE2325169A1 (de) | 1974-01-03 |
| SE396953B (sv) | 1977-10-10 |
| AU5702473A (en) | 1974-12-19 |
| FR2189431A1 (cs) | 1974-01-25 |
| CA1045296A (en) | 1978-12-26 |
| NL7307697A (cs) | 1973-12-18 |
| IT987928B (it) | 1975-03-20 |
| AU477290B2 (en) | 1976-10-21 |
| FR2189431B1 (cs) | 1977-09-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |